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NM_016010.3(ZC2HC1A):c.586G>A (p.Ala196Thr) AND not specified

Germline classification:
Likely benign (1 submission)
Last evaluated:
Feb 16, 2023
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV004262326.1

Allele description [Variation Report for NM_016010.3(ZC2HC1A):c.586G>A (p.Ala196Thr)]

NM_016010.3(ZC2HC1A):c.586G>A (p.Ala196Thr)

Genes:
IL7:interleukin 7 [Gene - OMIM - HGNC]
ZC2HC1A:zinc finger C2HC-type containing 1A [Gene - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8q21.13
Genomic location:
Preferred name:
NM_016010.3(ZC2HC1A):c.586G>A (p.Ala196Thr)
HGVS:
  • NC_000008.11:g.78697488G>A
  • NM_001362969.2:c.586G>A
  • NM_016010.3:c.586G>AMANE SELECT
  • NP_001349898.1:p.Ala196Thr
  • NP_057094.2:p.Ala196Thr
  • NC_000008.10:g.79609723G>A
  • NM_016010.2:c.586G>A
  • NR_156423.2:n.646G>A
Protein change:
A196T
Molecular consequence:
  • NM_001362969.2:c.586G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_016010.3:c.586G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_156423.2:n.646G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003879069Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Feb 16, 2023) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV003879069.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 26, 2024